Literature DB >> 31113236

Hydroxyurea Initiation Among Children With Sickle Cell Anemia.

Sarah L Reeves1, Hannah K Jary1, Jennifer P Gondhi1, Jean L Raphael2, Lynda D Lisabeth1, Kevin J Dombkowski1.   

Abstract

This study assesses characteristics of children with sickle cell anemia associated with hydroxyurea initiation. Medicaid administrative claims from 6 states (2005-2012) were used to identify children with sickle cell anemia enrolled in Medicaid for ≥2 years. Hydroxyurea use was defined as >30 days' supply of filled prescriptions. Children were classified as initiators (no use in year 1; use in year 2) or nonusers (no use in either year). Logistic regression was used to estimate associations between initiation, health care encounters, and demographics. A total of 4435 children were enrolled for 2 years during the study period; 885 (20.0%) initiators and 3080 (69.4%) nonusers. Children had an annual mean of 2.0 sickle cell disease-related inpatient admissions (SD = 2.2), 8.2 sickle cell disease-related outpatient visits (SD = 7.2), and 3.6 emergency department visits (SD = 3.5). The odds of initiating hydroxyurea increased with increasing health care utilization, age, and calendar year (all P values <.05).

Entities:  

Keywords:  administrative claims; hydroxyurea; medication; pain; sickle cell anemia

Mesh:

Substances:

Year:  2019        PMID: 31113236      PMCID: PMC7060659          DOI: 10.1177/0009922819850476

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  52 in total

1.  Adherence to hydroxyurea therapy in children with sickle cell anemia.

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3.  Study protocol for a randomized controlled trial to assess the feasibility of an open label intervention to improve hydroxyurea adherence in youth with sickle cell disease.

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Journal:  Contemp Clin Trials       Date:  2016-06-17       Impact factor: 2.226

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Authors:  Niti G Patel; Terianne Lindsey; Robert C Strunk; Michael R DeBaun
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5.  Persistence and compliance of deferoxamine versus deferasirox in Medicaid patients with sickle-cell disease.

Authors:  L B Jordan; F Vekeman; A Sengupta; M Corral; A Guo; M S Duh
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6.  Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease.

Authors:  Sean D Candrilli; Sarah H O'Brien; Russell E Ware; Milap C Nahata; Eric E Seiber; Rajesh Balkrishnan
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Review 7.  Understanding patient management: the need for medication adherence and persistence.

Authors:  Yc Chia
Journal:  Malays Fam Physician       Date:  2008-04-30

8.  Hydroxyurea use in Children with Sickle Cell Disease: Do Severely Affected Patients Use It and Does It Impact Hospitalization Outcomes?

Authors:  Susan E Creary; Deena J Chisolm; Terah L Koch; Victoria A Zigmont; Bo Lu; Sarah H O'Brien
Journal:  Pediatr Blood Cancer       Date:  2016-01-21       Impact factor: 3.167

9.  Provider barriers to hydroxyurea use in adults with sickle cell disease: a survey of the Sickle Cell Disease Adult Provider Network.

Authors:  Sophie Lanzkron; Carlton Haywood; Kathryn L Hassell; Cynthia Rand
Journal:  J Natl Med Assoc       Date:  2008-08       Impact factor: 1.798

10.  Technology Access and Smartphone App Preferences for Medication Adherence in Adolescents and Young Adults With Sickle Cell Disease.

Authors:  Sherif M Badawy; Alexis A Thompson; Robert I Liem
Journal:  Pediatr Blood Cancer       Date:  2016-02-04       Impact factor: 3.167

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  1 in total

1.  Impact of Medicaid expansion on access and healthcare among individuals with sickle cell disease.

Authors:  Mariam Kayle; Jhaqueline Valle; Susan Paulukonis; Jane L Holl; Paula Tanabe; Dustin D French; Ravi Garg; Robert I Liem; Sherif M Badawy; Marsha J Treadwell
Journal:  Pediatr Blood Cancer       Date:  2020-03-08       Impact factor: 3.167

  1 in total

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